GMP Training Courses - Regulatory Affairs

Handling Changes and Variations

Heidelberg, Germany

21/22 April 2020

Handling Changes and Variations

How to write the Quality Part of an IMPD

Prague, Czech Republic

13/14 May 2020

How to write the Quality Part of an IMPD

ICH Q12 - Product Life Cycle Management

Berlin, Germany

15/16 September 2020

ICH Q12 - Product Life Cycle Management

ICH Q12 Life Cycle Management & ICH 2/ICH Q14 Analytical Procedure Life Cycle Management

Berlin, Germany

15-17 September 2020

ICH Q12 Life Cycle Management & ICH 2/ICH Q14 Analytical Procedure Life Cycle Management

Drug Master File Procedures in the EU, the US and Japan

Vienna, Austria

29/30 September 2020

Drug Master File Procedures in the EU, the US and Japan

API Regulatory Starting Materials

Hamburg, Germany

13/14 October 2020

API Regulatory Starting Materials

GMP meets Regulatory Affairs

Hamburg, Germany

15/16 October 2020

GMP meets Regulatory Affairs

Blood and Plasma – Audits and Inspections

Berlin, Germany

27/28 October 2020

Blood and Plasma – Audits and Inspections

How to provide process validation data in regulatory submission

Hamburg, Germany

4/5 November 2020

How to provide process validation data in regulatory submission

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GMP Conferences by Topics

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